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Annona Species Monograph.pdf - Crops for the Future

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Chapter 8. Genetic Resources<br />

8.3 Ex situ conservation<br />

Ex situ conservation includes various strategies, such as seed storage, in vitro<br />

culture and field genebanking. <strong>Annona</strong> seeds show an orthodox response to<br />

desiccation and exposure to sub-zero temperatures. Cherimoya seeds tolerate<br />

desiccation to 4.8% moisture content, while soursop seeds tolerate<br />

desiccation to 5% moisture content. The seeds of sugar apple tolerate<br />

desiccation to 1.5% moisture content, and no viability loss occurred during 6<br />

months of hermetic storage at -20°C (Hong et al., 1996). These authors<br />

suggest that <strong>Annona</strong> seeds can be conserved in conventional seed genebanks<br />

under conditions of 18°C or less, in airtight containers at a seed moisture<br />

content of 5 ± 1%.<br />

In vitro culture techniques can be used <strong>for</strong> collecting, exchange and ex situ<br />

conservation of species that produce seedless fruits, as well as <strong>for</strong><br />

vegetatively propagated plants, including annonas. In vitro storage can be<br />

done by using slow growth techniques, when medium-term preservation is<br />

sufficient, or by cryopreservation in liquid nitrogen at -196°C, if <strong>the</strong> need is<br />

<strong>for</strong> long-term preservation. Both techniques present great advantages <strong>for</strong><br />

germplasm conservation. In vitro culture also offers <strong>the</strong> possibility of<br />

eliminating pathogens, and thus conserving and exchanging germplasm<br />

under disease free conditions. Despite <strong>the</strong>ir potential, in vitro conservation<br />

techniques are currently used to a limited extent only. This is due principally<br />

to <strong>the</strong> lack of research to develop protocols <strong>for</strong> each species (Ashmore,<br />

1997). Although several papers have appeared on annona tissue culture<br />

(Rasai et al., 1995; Lemos and Blake, 1996; Padilla, 1997; Castro et al.,<br />

1999; Encina et al., 1999; Lemos, 2000), a great deal of work remains to be<br />

done on development of methods <strong>for</strong> in vitro propagation <strong>for</strong> germplasm<br />

conservation of <strong>Annona</strong> species.<br />

Emphasis on in vitro research should be placed on conserving specific clonal<br />

material which is well documented. Much of <strong>the</strong> range of variation can be<br />

conserved using seed storage, and this is more cost-effective than attempting<br />

large in vitro programmes. Despite <strong>the</strong> availability of seed and in vitro<br />

conservation techniques, in practice <strong>the</strong> majority of <strong>Annona</strong> genetic resources<br />

are stored in field genebanks, also called clonal repositories or collections of<br />

living plants, which face higher risks of disease, human error and<br />

environmental hazards than o<strong>the</strong>r conservation techniques (Ferreira, 2001).<br />

These collections seem to be mainly breeders' collections, and are rarely<br />

representative of <strong>the</strong> range of <strong>Annona</strong> variability that needs to be conserved.<br />

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